Anti-obesity therapy for cardiovascular disease prevention: potential expected roles of glucagon-like peptide-1 receptor agonists

Cardiovasc Diabetol. 2022 Sep 6;21(1):176. doi: 10.1186/s12933-022-01611-8.

Abstract

Obesity is characterized by visceral fat accumulation and various metabolic disturbances that cause metabolic syndrome and obesity-related cardiovascular diseases (ORCVDs). Hence, treatments targeting obesity should also prevent ORCVDs. Nonetheless, lifestyle modification therapy alone is still insufficient to reduce the risk of ORCVDs, although most cardiovascular guidelines still list it as the only treatment for obesity. Additionally, conventional anti-obesity drugs, such as orlistat, phentermine-topiramate, and naltrexone-bupropion, can reduce body weight but have not demonstrated a clear reduction in the risk of ORCVDs. To overcome this unmet clinical need, newer anti-obesity drugs must exhibit not only sufficient and long-lasting weight loss but also obvious cardiovascular benefits. Given recent clinical findings and evidences, in this context glucagon-like peptide-1 receptor agonist is currently available as a candidate that is clinically positioned as a first-line anti-obesity agent for the effective prevention of ORCVDs in people with obesity.

Keywords: Anti-obesity; Glucagon-like peptide-1 receptor agonists; Liraglutide; Obesity-related cardiovascular disease; Semaglutide.

MeSH terms

  • Anti-Obesity Agents* / adverse effects
  • Cardiovascular Diseases* / diagnosis
  • Cardiovascular Diseases* / epidemiology
  • Cardiovascular Diseases* / prevention & control
  • Glucagon-Like Peptide-1 Receptor / agonists
  • Humans
  • Liraglutide / therapeutic use
  • Obesity / diagnosis
  • Obesity / drug therapy
  • Obesity / epidemiology
  • Orlistat / therapeutic use

Substances

  • Anti-Obesity Agents
  • Glucagon-Like Peptide-1 Receptor
  • Liraglutide
  • Orlistat